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Pediatric Formulations

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Release : 2014-01-30
Genre : Medical
Kind : eBook
Book Rating : 113/5 ( reviews)

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Book Synopsis Pediatric Formulations by : Daniel Bar-Shalom

Download or read book Pediatric Formulations written by Daniel Bar-Shalom. This book was released on 2014-01-30. Available in PDF, EPUB and Kindle. Book excerpt: Until the 1990s, it was generally accepted that medicines were first developed for adults and their use in children was investigated later, if at all. One of the main tasks of hospital pharmacies was the manufacturing of child-appropriate formulations in a more or less makeshift way. The first change came in 1997 with U.S. legislation that rewarded manufacturers to do voluntary pediatric research. Ten years later, the European Union passed legislation that required manufacturers to discuss all pediatric aspects, including formulations, with the regulatory authorities as a condition of starting the registration procedure. In consequence, manufacturers must now cover all age groups, including the youngest ones. So far, pediatric formulations were more a focus for academic researchers. Through the changed regulatory environment, there is now a sudden high commercial demand for age-appropriate formulations. This book begins by highlighting the anatomical, physiological and developmental differences between adults and children of different ages. It goes on to review the existing technologies and attempts to draw a roadmap to better, innovative formulations, in particular for oral administration. The regulatory, clinical, ethical and pharmaceutical framework is also addressed.

Paediatric Formulation

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Author :
Release : 2021-09-02
Genre : Science
Kind : eBook
Book Rating : 40X/5 ( reviews)

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Book Synopsis Paediatric Formulation by : Nunzio Denora

Download or read book Paediatric Formulation written by Nunzio Denora. This book was released on 2021-09-02. Available in PDF, EPUB and Kindle. Book excerpt: The development of paediatric medicines can be challenging since this is a different patient population with specific needs. A medicine designed for use in paediatric patients must consider the following aspects: patient population variability; the need for dose flexibility; route of administration; patient compliance; excipient tolerability. For example, the toxicity of excipients may differ in children compared to adults and children have different taste preferences. Globally, about 75% of drugs do not carry regulatory approval for use in children; worldwide, many medications prescribed for the treatment of paediatric diseases are used off-label, and less than 20% of package inserts have sufficient information for treating children. This book provides an update on both state-of-the-art methodology and operational challenges in paediatric formulation design and development. It aims at re-evaluating what is needed for more progress in the design and development of age-appropriate treatments for paediatric diseases, focusing on: formulation development; drug delivery design; efficacy, safety, and tolerability of drugs and excipients.

Pediatric Drug Formulations

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Author :
Release : 2014-01-01
Genre : Medical
Kind : eBook
Book Rating : 144/5 ( reviews)

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Book Synopsis Pediatric Drug Formulations by : Milap Nahata

Download or read book Pediatric Drug Formulations written by Milap Nahata. This book was released on 2014-01-01. Available in PDF, EPUB and Kindle. Book excerpt:

Safe and Effective Medicines for Children

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Author :
Release : 2012-10-13
Genre : Medical
Kind : eBook
Book Rating : 493/5 ( reviews)

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Book Synopsis Safe and Effective Medicines for Children by : Institute of Medicine

Download or read book Safe and Effective Medicines for Children written by Institute of Medicine. This book was released on 2012-10-13. Available in PDF, EPUB and Kindle. Book excerpt: The Best Pharmaceuticals for Children Act (BPCA) and the Pediatric Research Equity Act (PREA) were designed to encourage more pediatric studies of drugs used for children. The FDA asked the IOM to review aspects of pediatric studies and changes in product labeling that resulted from BPCA and PREA and their predecessor policies, as well as assess the incentives for pediatric studies of biologics and the extent to which biologics have been studied in children. The IOM committee concludes that these policies have helped provide clinicians who care for children with better information about the efficacy, safety, and appropriate prescribing of drugs. The IOM suggests that more can be done to increase knowledge about drugs used by children and thereby improve the clinical care, health, and well-being of the nation's children.

Paediatric Formulation: Design and Development

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Author :
Release : 2021
Genre :
Kind : eBook
Book Rating : 415/5 ( reviews)

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Book Synopsis Paediatric Formulation: Design and Development by : Nunzio Denora

Download or read book Paediatric Formulation: Design and Development written by Nunzio Denora. This book was released on 2021. Available in PDF, EPUB and Kindle. Book excerpt: The development of paediatric medicines can be challenging since this is a different patient population with specific needs. A medicine designed for use in paediatric patients must consider the following aspects: patient population variability; the need for dose flexibility; route of administration; patient compliance; excipient tolerability. For example, the toxicity of excipients may differ in children compared to adults and children have different taste preferences. Globally, about 75% of drugs do not carry regulatory approval for use in children; worldwide, many medications prescribed for the treatment of paediatric diseases are used off-label, and less than 20% of package inserts have sufficient information for treating children. This book provides an update on both state-of-the-art methodology and operational challenges in paediatric formulation design and development. It aims at re-evaluating what is needed for more progress in the design and development of age-appropriate treatments for paediatric diseases, focusing on: formulation development; drug delivery design; efficacy, safety, and tolerability of drugs and excipients.

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